Undecane

Details

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Internal ID c53325a3-5d3a-44a8-8e56-8b38f09c3357
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name undecane
SMILES (Canonical) CCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCC
InChI InChI=1S/C11H24/c1-3-5-7-9-11-10-8-6-4-2/h3-11H2,1-2H3
InChI Key RSJKGSCJYJTIGS-UHFFFAOYSA-N
Popularity 2,833 references in papers

Physical and Chemical Properties

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Molecular Formula C11H24
Molecular Weight 156.31 g/mol
Exact Mass 156.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.54
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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N-UNDECANE
1120-21-4
Hendecane
Decane, methyl-
CCRIS 3796
Hendekan
Undekan
HSDB 5791
UNII-JV0QT00NUE
JV0QT00NUE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Undecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9762 97.62%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8443 84.43%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8413 84.13%
P-glycoprotein inhibitior - 0.9631 96.31%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.7947 79.47%
CYP2C9 substrate - 0.8415 84.15%
CYP2D6 substrate - 0.7215 72.15%
CYP3A4 inhibition - 0.9877 98.77%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9540 95.40%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.6175 61.75%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.8149 81.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6328 63.28%
Eye corrosion + 0.9946 99.46%
Eye irritation + 0.9955 99.55%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.9874 98.74%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6573 65.73%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8836 88.36%
skin sensitisation + 0.9563 95.63%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.6948 69.48%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6552 65.52%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding - 0.9410 94.10%
Androgen receptor binding - 0.8512 85.12%
Thyroid receptor binding - 0.7488 74.88%
Glucocorticoid receptor binding - 0.9131 91.31%
Aromatase binding - 0.9055 90.55%
PPAR gamma - 0.8681 86.81%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity + 0.8690 86.90%
Fish aquatic toxicity + 0.9770 97.70%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.23% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.92% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 91.78% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.44% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.59% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.52% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.15% 85.94%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 83.58% 90.24%
CHEMBL2996 Q05655 Protein kinase C delta 83.44% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.77% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Allium ampeloprasum
Ammodendron karelinii
Anacyclus pyrethrum
Angelica acutiloba
Angelica gigas
Angelica sinensis
Anthriscus cerefolium
Araucaria cunninghamii
Aristolochia gigantea
Asarum megacalyx
Aster tataricus
Astilbe rubra
Atractylodes lancea
Atractylodes macrocephala
Bellis perennis
Brachylaena perrieri
Brassica napus
Buglossoides arvensis
Cannabis sativa
Caryocar coriaceum
Centaurea benedicta
Chaenomeles sinensis
Chrysanthemum indicum
Cistus creticus
Cistus monspeliensis
Clinopodium suaveolens
Combretum indicum
Crinum jagus
Curcuma longa
Cuscuta australis
Daphne odora
Dendrobium chrysanthum
Diplotropis ferruginea
Ducrosia ismaelis
Elettaria cardamomum
Elsholtzia ciliata
Endopappus macrocarpus subsp. macrocarpus
Etlingera elatior
Eucalyptus viminalis
Euphrasia regelii
Glycyrrhiza glabra
Hamamelis virginiana
Hortonia angustifolia
Houttuynia cordata
Hypericum perforatum
Hypericum rumeliacum
Hypericum triquetrifolium
Illicium difengpi
Juglans nigra
Julbernardia globiflora
Juniperus chinensis
Laggera crispata
Lantana camara
Lycium barbarum
Lycium chinense
Medicosma fareana
Meiogyne virgata
Mentha longifolia subsp. longifolia
Micromeria myrtifolia
Miliusa balansae
Mimusops laurifolia
Mosla chinensis
Myrrhis odorata
Nepeta racemosa
Origanum vulgare
Othonna macrophylla
Pentachondra pumila
Persicaria minor
Phagnalon rupestre
Phlomoides ostrowskiana
Phlox paniculata
Phyllanthus emblica
Piliostigma thonningii
Pimpinella anisum
Pimpinella peregrina
Pinus flexilis
Pinus koraiensis
Pinus lambertiana
Pinus monticola
Pinus ponderosa
Proiphys amboinensis
Rosa multiflora
Salix petiolaris
Salvia caespitosa
Salvia lanigera
Salvia pisidica
Sauromatum venosum
Scutellaria baicalensis
Senecio isatideus
Senecio nemorensis
Senna alexandrina
Solanum crinitum
Trigonella foenum-graecum
Tubocapsicum anomalum
Uncaria longiflora
Ursinia speciosa
Vaccinium angustifolium

Cross-Links

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PubChem 14257
NPASS NPC82648
LOTUS LTS0081068
wikiData Q150731